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2,3,4,8,9-pentafluoro-12H-benzimidazo[2,1-b][1,3]benzothiazin-12-one | 639088-54-3

中文名称
——
中文别名
——
英文名称
2,3,4,8,9-pentafluoro-12H-benzimidazo[2,1-b][1,3]benzothiazin-12-one
英文别名
2,3,4,8,9-pentafluorobenzimidazolo[2,1-b][1,3]benzothiazin-12-one
2,3,4,8,9-pentafluoro-12H-benzimidazo[2,1-b][1,3]benzothiazin-12-one化学式
CAS
639088-54-3
化学式
C14H3F5N2OS
mdl
MFCD05259924
分子量
342.249
InChiKey
RDCPHQGMEHPUNK-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4
  • 重原子数:
    23
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    60.2
  • 氢给体数:
    0
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    四氢吡咯2,3,4,8,9-pentafluoro-12H-benzimidazo[2,1-b][1,3]benzothiazin-12-one吡啶 为溶剂, 反应 5.0h, 以85%的产率得到
    参考文献:
    名称:
    摘要:
    The heating of derivatives of benzimidazole-2-thione and imidazolidine-2-thione with tetra- (penta)fluorobenzoyl chlorides in toluene or pyridine gave rise to fluorocontaining derivatives of imidazo[2,1-b][1,3]benzothiazine. The latter were studied in reactions of nucleophilic substitution of fluorine for amino groups.
    DOI:
    10.1023/a:1025548505109
  • 作为产物:
    参考文献:
    名称:
    摘要:
    The heating of derivatives of benzimidazole-2-thione and imidazolidine-2-thione with tetra- (penta)fluorobenzoyl chlorides in toluene or pyridine gave rise to fluorocontaining derivatives of imidazo[2,1-b][1,3]benzothiazine. The latter were studied in reactions of nucleophilic substitution of fluorine for amino groups.
    DOI:
    10.1023/a:1025548505109
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文献信息

  • ——
    作者:G. N. Lipunova、E. V. Nosova、G. A. Mokrushina、E. G. Ogloblina、G. G. Aleksandrov、V. N. Charushin
    DOI:10.1023/a:1025548505109
    日期:——
    The heating of derivatives of benzimidazole-2-thione and imidazolidine-2-thione with tetra- (penta)fluorobenzoyl chlorides in toluene or pyridine gave rise to fluorocontaining derivatives of imidazo[2,1-b][1,3]benzothiazine. The latter were studied in reactions of nucleophilic substitution of fluorine for amino groups.
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